ALDH1 expression predicts progression of premalignant lesions to cancer in Type I endometrial carcinomas

Abstract In type 1 endometrial cancer, unopposed estrogen stimulation is thought to lead to endometrial hyperplasia which precedes malignant progression. Recent data from our group and others suggest that ALDH activity mediates stemness in endometrial cancer, but while aldehyde dehydrogenase 1 (ALDH...

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Autores principales: Vei Mah, Yahya Elshimali, Alison Chu, Neda A. Moatamed, Jamar P. Uzzell, Jessica Tsui, Stephen Schettler, Hania Shakeri, Madhuri Wadehra
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:a4999bcdf8744e5fbea3ffe78e4fe2a32021-12-02T17:52:23ZALDH1 expression predicts progression of premalignant lesions to cancer in Type I endometrial carcinomas10.1038/s41598-021-90570-32045-2322https://doaj.org/article/a4999bcdf8744e5fbea3ffe78e4fe2a32021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-90570-3https://doaj.org/toc/2045-2322Abstract In type 1 endometrial cancer, unopposed estrogen stimulation is thought to lead to endometrial hyperplasia which precedes malignant progression. Recent data from our group and others suggest that ALDH activity mediates stemness in endometrial cancer, but while aldehyde dehydrogenase 1 (ALDH1) has been suggested as a putative cancer stem cell marker in several cancer types, its clinical and prognostic value in endometrial cancer remains debated. The aim of this study was to investigate the clinical value of ALDH1 expression in endometrial hyperplasia and to determine its ability to predict progression to endometrial cancer. Interrogation of the TCGA database revealed upregulation of several isoforms in endometrial cancer, of which the ALDH1 isoforms collectively constituted the largest group. To translate its expression, a tissue microarray was previously constructed which contained a wide sampling of benign and malignant endometrial samples. The array contained a metachronous cohort of samples from individuals who either developed or did not develop endometrial cancer. Immunohistochemical staining was used to determine the intensity and frequency of ALDH1 expression. While benign proliferative and secretory endometrium showed very low levels of ALDH1, slightly higher expression was observed within the stratum basalis. In disease progression, cytoplasmic ALDH1 expression showed a step-wise increase between endometrial hyperplasia, atypical hyperplasia, and endometrial cancer. ALDH1 was also shown to be an early predictor of EC development, suggesting that it can serve as an independent prognostic indicator of patients with endometrial hyperplasia with or without atypia who would progress to cancer (p = 0.012).Vei MahYahya ElshimaliAlison ChuNeda A. MoatamedJamar P. UzzellJessica TsuiStephen SchettlerHania ShakeriMadhuri WadehraNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Vei Mah
Yahya Elshimali
Alison Chu
Neda A. Moatamed
Jamar P. Uzzell
Jessica Tsui
Stephen Schettler
Hania Shakeri
Madhuri Wadehra
ALDH1 expression predicts progression of premalignant lesions to cancer in Type I endometrial carcinomas
description Abstract In type 1 endometrial cancer, unopposed estrogen stimulation is thought to lead to endometrial hyperplasia which precedes malignant progression. Recent data from our group and others suggest that ALDH activity mediates stemness in endometrial cancer, but while aldehyde dehydrogenase 1 (ALDH1) has been suggested as a putative cancer stem cell marker in several cancer types, its clinical and prognostic value in endometrial cancer remains debated. The aim of this study was to investigate the clinical value of ALDH1 expression in endometrial hyperplasia and to determine its ability to predict progression to endometrial cancer. Interrogation of the TCGA database revealed upregulation of several isoforms in endometrial cancer, of which the ALDH1 isoforms collectively constituted the largest group. To translate its expression, a tissue microarray was previously constructed which contained a wide sampling of benign and malignant endometrial samples. The array contained a metachronous cohort of samples from individuals who either developed or did not develop endometrial cancer. Immunohistochemical staining was used to determine the intensity and frequency of ALDH1 expression. While benign proliferative and secretory endometrium showed very low levels of ALDH1, slightly higher expression was observed within the stratum basalis. In disease progression, cytoplasmic ALDH1 expression showed a step-wise increase between endometrial hyperplasia, atypical hyperplasia, and endometrial cancer. ALDH1 was also shown to be an early predictor of EC development, suggesting that it can serve as an independent prognostic indicator of patients with endometrial hyperplasia with or without atypia who would progress to cancer (p = 0.012).
format article
author Vei Mah
Yahya Elshimali
Alison Chu
Neda A. Moatamed
Jamar P. Uzzell
Jessica Tsui
Stephen Schettler
Hania Shakeri
Madhuri Wadehra
author_facet Vei Mah
Yahya Elshimali
Alison Chu
Neda A. Moatamed
Jamar P. Uzzell
Jessica Tsui
Stephen Schettler
Hania Shakeri
Madhuri Wadehra
author_sort Vei Mah
title ALDH1 expression predicts progression of premalignant lesions to cancer in Type I endometrial carcinomas
title_short ALDH1 expression predicts progression of premalignant lesions to cancer in Type I endometrial carcinomas
title_full ALDH1 expression predicts progression of premalignant lesions to cancer in Type I endometrial carcinomas
title_fullStr ALDH1 expression predicts progression of premalignant lesions to cancer in Type I endometrial carcinomas
title_full_unstemmed ALDH1 expression predicts progression of premalignant lesions to cancer in Type I endometrial carcinomas
title_sort aldh1 expression predicts progression of premalignant lesions to cancer in type i endometrial carcinomas
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/a4999bcdf8744e5fbea3ffe78e4fe2a3
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